A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697832



Internal ID121498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69348632..69349382hg38UCSC Ensembl
chr14:69815349..69816099hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498451
Supporting Variants
Samples
Known GenesGALNT16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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